Skip to content

Comparative evaluation of the effect of Gluma Desensitizer and high power 980-nm Diode Laser and combination of them on reduction of dentin hypersensitivity

Comparative evaluation of the effect of Gluma Desensitizer and high power Diode Laser 980-nm and combination use of them on reduction of dentin hypersensitivity

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20120901010703N5
Enrollment
20
Registered
2022-02-24
Start date
2022-01-20
Completion date
Unknown
Last updated
2022-03-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dentin hypersensitivity. Other specified diseases of hard tissues of teeth

Interventions

Intervention 1: Intervention group: intervention group 1 treatment with gluma desensitizer from Kulzer Company.gluma desensitizer apply on dry teeth 60 seconds and dry for 5 secondes. Intervention 2:

Sponsors

Esfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients referred to the general and specialized periodontics department of Isfahan Dental School have 3 teeth with complaints of cervical dentin sensitivity and sensitivity to cold stimuli that are not adjacent to each other. Patients should be available for three months during the study period and sign the informed consent form .Teeth do not need restorative treatment People over 18 years old

Exclusion criteria

Exclusion criteria: Caries, crack and pulpitis, Existence of active caries, cervically restored teeth, coronary fractures .Pregnant and lactating people smoking Patients and who have used anti-sensitive toothpaste and other medicines for the past 6 months. bleaching in past 6 months, diet (use of sour and acidic foods), People who have high O'leary index in follow up sessions (higher than 25%)

Design outcomes

Primary

MeasureTime frame
Amount of patient's pain (dentin hypersensitivity). Timepoint: Before treatment, 15 minutes after treatment in the first session, one week after the first session, two weeks after the first session, one month after the first session, tree months after the first session. Method of measurement: Use of cold spray, use of air syringe of unit.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNarges Naghsh

Esfahan University of Medical Sciences

n_naghsh@dnt.mui.ac.ir+98 31 1792 2870

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 8, 2026